rnf5[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 13

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	RNF5, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	RNF5, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	RNF5, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	RNF5, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	RNF5, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	RNF5, TRR-ACG1-2, 1385 more genes
nsv4675941	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055	RNF5, AGER, 217 more genes
nsv7097426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173	RNF5, LEMD2, 321 more genes
nsv7098787	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173	RNF5, CUTA, 184 more genes
nsv4455450	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,027,371-32,448,599 , GRCh38.p12 chr6: 32,059,594-32,480,822	RNF5, AGPAT1, 23 more genes
nsv4675453	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 31,916,915-32,278,000 , GRCh38.p12 chr6: 31,949,138-32,310,223	RNF5, NOTCH4, 29 more genes
nsv3886007	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 31,952,482-32,243,155 , GRCh38.p12 chr6: 31,984,705-32,275,378	RNF5, STK19B, 22 more genes
nsv3884305	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,052,479-32,184,403 , GRCh38.p12 chr6: 32,084,702-32,216,626	RNF5, PRRT1, 14 more genes

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